Author
J. J. Gokey
Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.
Biology Disciplines
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2021-2023 · peak 5/yrCo-Author Collaboration Network
10 top collaborators · 41 mutual co-author links6 papers
Recent·Most cited
- Cell BiologybioRxiv
Epithelial Yap/Taz are required for functional alveolar regeneration following acute lung injury
G. T. DiGiovanni, W. Han, T. Sherrill…·J. J. Gokey
This study shows that Yap/Taz in AT2 cells are essential for alveolar regeneration and preventing fibrosis after lung injury.
DOI 10.1172/jci.insight.173374 - Cell BiologybioRxiv
Dysregulated alveolar epithelial cell progenitor function and identity in Hermansky-Pudlak syndrome
J. Y. Wang, N. S. Michki, S. Sitaraman…·L. R. Young
This study identifies intrinsic AT2 progenitor dysfunction and p53 pathway dysregulation as novel mechanisms driving pulmonary fibrosis in Hermansky-Pudlak syndrome.
DOI 10.1172/jci.insight.183483 - Cell BiologybioRxivPreprint
Myeloid Cell-Derived IL1β Contributes to Pulmonary Vascular Remodeling in Heart Failure with Preserved Ejection Fraction
V. Agrawal, J. A. Kropski, J. J. Gokey…·A. R. Hemnes
This study identifies myeloid cell-derived IL1β as a key driver of pulmonary vascular remodeling in HFpEF using a murine model and multi-omics approaches.
DOI 10.1101/2023.05.18.541302 - PathologybioRxiv
Repetitive Sulfur Dioxide Exposure in Mice Models Post-Deployment Respiratory Syndrome
S. S. Gutor, R. I. Salinas, D. S. Nichols…·V. V. Polosukhin
This study develops a mouse model of repetitive sulfur dioxide exposure that mimics post-deployment respiratory syndrome features, identifying oxidative stress as a mediator of pulmonary vascular disease.
DOI 10.1152/ajplung.00239.2023 - Cell BiologybioRxivPreprint
Single-cell transcriptomic assessment of cellular phenotype stability in human precision-cut lung slices
N. I. Winters, C. J. Taylor, C. S. Jetter…·J. A. Kropski
The paper compares single-cell transcriptomic profiles of human PCLS after five days of culture to freshly isolated lung tissue, finding changes in endothelial and alveolar epithelial cell programs but stable immune cell profiles.